Canonical Allele Identifier: PA2830235732
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202845
ClinVar RCV Id: RCV000472425 RCV001704917 RCV002336482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Thr15403Ser
CA310463
NM_133437.4:c.46207A>T
CA349645266
NM_133437.4:c.46208C>G